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临床试验/TCTR20200128007
TCTR20200128007已完成4 期

POSTOPERATIVE PAIN MANAGEMENT USING BUPIVACAINE AFTER MANDIBULAR ORTHOGNATHIC SURGERY: A TRIPLE-BLINDED RANDOMIZED CONTROLLED CLINICAL TRIA

Faculty of Dentistry, Mahidol University, Thailand0 个研究点目标入组 28 人开始时间: 2020年1月28日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
28

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 45 Years(—)
性别
All

入选标准

  • 1. American Society of Anesthesiologist (ASA): class I and II
  • 2. Patients undergoing Bilateral Sagittal Split Osteotomy (BSSRO) of mandible
  • only without complication.
  • - Mandibular advancement or setback

排除标准

  • 1. All the patients with any history of allergy to local anesthetics, opioid, NSAID or any of the
  • medications being administered.
  • 2. Patients with a history of narcotic or alcohol abuse.
  • 3. Patients with a history of chronic debilitating disease.
  • 4. Chronic opioid analgesic use.
  • 5. Pregnancy and lactating mother.
  • 6. Patients undergoing both jaw surgery (lefort 1 + BSSRO) or Lefort 1 only

研究者

发起方
Faculty of Dentistry, Mahidol University, Thailand

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